Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.ppat.1004972
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dc.titleTwilight, a Novel Circadian-Regulated Gene, Integrates Phototropism with Nutrient and Redox Homeostasis during Fungal Development
dc.contributor.authorDeng Y.Z.
dc.contributor.authorQu Z.
dc.contributor.authorNaqvi N.I.
dc.date.accessioned2020-03-13T05:24:12Z
dc.date.available2020-03-13T05:24:12Z
dc.date.issued2015
dc.identifier.citationDeng Y.Z., Qu Z., Naqvi N.I. (2015). Twilight, a Novel Circadian-Regulated Gene, Integrates Phototropism with Nutrient and Redox Homeostasis during Fungal Development. PLoS Pathogens 11 (6) : e1004972. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.ppat.1004972
dc.identifier.issn15537366
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/165390
dc.description.abstractPhototropic regulation of circadian clock is important for environmental adaptation, organismal growth and differentiation. Light plays a critical role in fungal development and virulence. However, it is unclear what governs the intracellular metabolic response to such dark-light rhythms in fungi. Here, we describe a novel circadian-regulated Twilight (TWL) function essential for phototropic induction of asexual development and pathogenesis in the rice-blast fungus Magnaporthe oryzae. The TWL transcript oscillates during circadian cycles and peaks at subjective twilight. GFP-Twl remains acetylated and cytosolic in the dark, whereas light-induced phosphorylation (by the carbon sensor Snf1 kinase) drives it into the nucleus. The mRNA level of the transcription/repair factor TFB5, was significantly down regulated in the twl∆ mutant. Overexpression of TFB5 significantly suppressed the conidiation defects in the twl∆ mutant. Furthermore, Tfb5-GFP translocates to the nucleus during the phototropic response and under redox stress, while it failed to do so in the twl∆ mutant. Thus, we provide mechanistic insight into Twl-based regulation of nutrient and redox homeostasis in response to light during pathogen adaptation to the host milieu in the rice blast pathosystem. © 2015 Deng et al.
dc.publisherPublic Library of Science
dc.sourceUnpaywall 20200320
dc.subjecttranscription factor SNF
dc.subjectfungal protein
dc.subjectacetylation
dc.subjectArticle
dc.subjectcircadian rhythm
dc.subjectcontrolled study
dc.subjectdarkness
dc.subjectfungal development
dc.subjectfungal gene
dc.subjectfungal metabolism
dc.subjectgenetic regulation
dc.subjecthabitual adaptation
dc.subjecthomeostasis
dc.subjectMagnaporthe oryzae
dc.subjectnonhuman
dc.subjectphosphorylation
dc.subjectphototropism
dc.subjectTwilight gene
dc.subjectcircadian rhythm
dc.subjectdrug effects
dc.subjectfood
dc.subjectfungus hyphae
dc.subjectfungus spore
dc.subjectgene expression regulation
dc.subjectgenetics
dc.subjectgrowth, development and aging
dc.subjecthomeostasis
dc.subjectlight
dc.subjectMagnaporthe
dc.subjectmetabolism
dc.subjectmicrobiology
dc.subjectOryza
dc.subjectoxidation reduction reaction
dc.subjectphototropism
dc.subjectphysiology
dc.subjectplant disease
dc.subjectFungi
dc.subjectMagnaporthe grisea
dc.subjectMagnaporthe oryzae
dc.subjectCircadian Rhythm
dc.subjectFood
dc.subjectFungal Proteins
dc.subjectGene Expression Regulation, Fungal
dc.subjectHomeostasis
dc.subjectHyphae
dc.subjectLight
dc.subjectMagnaporthe
dc.subjectOryza
dc.subjectOxidation-Reduction
dc.subjectPhototropism
dc.subjectPlant Diseases
dc.subjectSpores, Fungal
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1371/journal.ppat.1004972
dc.description.sourcetitlePLoS Pathogens
dc.description.volume11
dc.description.issue6
dc.description.pagee1004972
dc.published.statePublished
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